Emcure Pharmaceuticals is hiring Officer/Executive/AM for QC Microbiology Department Emcure Pharmaceuticals is looking for dedicated and detail-oriented professionals for QC Microbiology team. Details are provided below 1. Position:Officer/Executive / AM 2. Job Location: Sanand, Ahmedabad 3. Experience: 2 to 8 Years 5. Department: QC Micro 6. Qualification: B.Sc./M.Sc. Microbiology (or) B.Pharm / M.Pharm 7. Key areas of Work : -Water Testing: Perform analysis of purified-water, WFI, potable water and water for injection as per IP/USP/EP guidelines. -Sterility Testing: Perform sterility testing of pharmaceutical products, raw materials and components as per IP/USP. -Microbial Limit Testing (MLT): Conduct microbial limit tests of raw materials, in-process and finished products. -Environmental Monitoring (EM): Perform monitoring of viable and non-viable particles in clean areas as per SOP -Media & Reagent Preparation: Prepare, sterilize and per...
Vacancy in Bioprocess Upstream & Downstream (Bacterial Vaccine Production) - B.Sc / M.Sc /B.Tech (Biotech, Microbiology, Biochemistry, or related)
Bharat Biotech International Limited for Bioprocess Production Team (Upstream & Downstream) at Genome Valley, Hyderabad.
If you or someone you know has relevant experience in vaccine or biopharma production, you can apply!
Position: Bioprocess Upstream & Downstream (Bacterial Vaccine Production)
Location: Hyderabad
Experience: 3 to 8 years
Qualification: B.Sc / M.Sc /B.Tech (Biotech, Microbiology, Biochemistry, or related)
Apply at: "kiran4978@bharatbiotech.com"
Note: Suitable candidates will be contacted.
Key Responsibilities
Upstream Production:
Operation of bioreactors, fermenters, and incubators
Media preparation and cell culture handling
Monitoring pH, DO, temperature, agitation, etc.
Downstream Production:
Handling centrifuges, TFF systems, chromatography skids, and filtration units
Execution of purification processes (e.g., affinity, ion exchange)
Buffer preparation and CIP/SIP of equipment
General:
Documentation and compliance with GMP, SOPs, and safety protocols
Requirements Hands-on experience in vaccine/biopharma production processes
Knowledge of GMP, GDP, and cleanroom operations
Willing to work in shifts and controlled environments
Strong understanding of equipment and process parameters
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